Hyperlipidemia Clinical Trial
Official title:
Red Yeast Rice and Phytosterols Versus Red Yeast Rice and Placebo for the Treatment of Hyperlipidemia in Patients With Statin Intolerance: A Multi-Center Randomized Double-blind Study
Verified date | November 2009 |
Source | Chestnut Hill Health System |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Red yeast rice may be useful to lower cholesterol, especially in a population of patients who
cannot tolerate traditional therapy with statins.
The addition of an over-the-counter phytosterol to red yeast rice may offer additional lipid
lowering benefits when compared to red yeast rice alone.
These supplements will be given to all participants. Up to one-half will enroll in a
lifestyle intervention program called Change of Heart and will be compared to patients who do
not participate in the program. The study will last one year.
Status | Completed |
Enrollment | 200 |
Est. completion date | July 2011 |
Est. primary completion date | November 2010 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 21 Years and older |
Eligibility |
Inclusion Criteria: - Men and women age > 21 - LDL > 100 and physician suggestion to take statin - Subject complains of muscle weakness or aching which he/she or his/her physician feels may be attributable to statin therapy - Having stopped a statin drug for personal reasons and not willing to restart this medication - Refusal to take a statin as prescribed by personal physician - CPK < 400 - Not taking any cholesterol lowering medication, red yeast rice extract or a phytosterol product for at least 1 month prior to initiation of trial - Ability to exercise without physical restrictions - Ability to attend 12 week consecutive Change of Heart lifestyle education sessions - Liver function studies normal at baseline - Subject willing to remain off the dietary supplement CoQ10 for duration of trial - TSH must be normal Exclusion Criteria: - A history of muscle damage (CPK > 400 IU) on statin therapy - Any active cardiac problem including chest pain, angina, shortness of breath with minimal activity, or unstable angina/acute coronary syndrome within one year - Known intolerance to one of the study drugs - Physical limitation preventing aerobic exercise program, such as severe arthritis, peripheral vascular disease, congestive heart failure, or symptom limiting pulmonary disease - Uncontrolled hypertension (defined as SBP > 180 mmHg or DBP > 100 mmHg - Heart attack, bypass surgery, or angioplasty/stent within 1 year of study - Triglyceride level more than 400 mg/dl - Underlying musculoskeletal disorder preventing muscle testing - Taking other medicines including: cyclosporine, erythromycin or other macrolide antibiotics; fluconazole; niacin; fibrates; or > 16 oz. of grapefruit juice daily |
Country | Name | City | State |
---|---|---|---|
United States | Abington Memorial Hospital | Abington | Pennsylvania |
United States | Chestnut Hill Hospital | Philadelphia | Pennsylvania |
Lead Sponsor | Collaborator |
---|---|
Chestnut Hill Health System |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | LDL cholesterol levels | one year | ||
Secondary | myalgia compared to prior statin usage | one year | ||
Secondary | other lipoprotein levels | one year | ||
Secondary | weight loss in TLC program vs. baseline | one year |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT00001154 -
Lipoprotein Metabolism in Normal Volunteers and Patients With High Levels of Lipoproteins
|
||
Completed |
NCT02927184 -
Safety and Tolerability of VK2809 in Patients With Primary Hypercholesterolemia and Non-Alcoholic Fatty Liver Disease
|
Phase 2 | |
Completed |
NCT04640012 -
Ascending-Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics of DC371739 Single-Dose Treatment in Healthy Subjects
|
Phase 1 | |
Completed |
NCT03213288 -
Bilberry Fruit and Black Rice Derived Anthocyanins on Lipid Status
|
N/A | |
Completed |
NCT00382564 -
Magnetic Resonance Angiography to Diagnose Atherosclerotic Disease
|
N/A | |
Recruiting |
NCT02979704 -
A Comparative Study of Rosuvastatin and Atorvastatin in Patients With Hyperlipidemia
|
Phase 2/Phase 3 | |
Completed |
NCT02569814 -
A Study to Compare the Pharmacokinetics and Safety of a Fixed Dose Combination of Fimasartan/Amlodipine/Rosuvastatin
|
Phase 1 | |
Completed |
NCT02280590 -
Comparison of the Efficacy and Safety of Cresnon® and Crestor® in Patients With Hyperlipidemia
|
Phase 4 | |
Completed |
NCT02428998 -
Safety for 24 Weeks Intake of Korean Red Ginseng in Adults
|
N/A | |
Completed |
NCT01678183 -
Financial Incentives for Medication Adherence
|
N/A | |
Completed |
NCT01694446 -
Regulation of Intestinal and Hepatic Lipoprotein Production by Glucose and Fructose
|
N/A | |
Completed |
NCT01426412 -
A Study of LY3015014 in Healthy Participants With Elevated Low Density Lipoprotein Cholesterol
|
Phase 1 | |
Completed |
NCT01131832 -
Genetic Basis for Heterogeneity in Response of Plasma Lipids to Plant Sterols
|
Phase 4 | |
Completed |
NCT00534105 -
Lipid Metabolism in Gestational Diabetes
|
N/A | |
Completed |
NCT00758303 -
A Study to Evaluate the Lipid Regulating Effects of TRIA-662
|
Phase 2/Phase 3 | |
Recruiting |
NCT00408824 -
Investigation of Genetic Risk of Metabolic Syndrome in Company Employee (NGK Study)
|
N/A | |
Completed |
NCT00362206 -
Comparison of the Combination of Fenofibrate and Simvastatin Versus Pravastatin
|
Phase 3 | |
Terminated |
NCT00299169 -
Randomized Trial Comparing N of 1 Trials to Standard Practice to Improve Adherence to Statins in Patients With Diabetes
|
Phase 4 | |
Completed |
NCT00414986 -
Using Learning Teams for Reflective Adaptation for Diabetes and Depression
|
N/A | |
Completed |
NCT00381992 -
Risk Assessment of Long-Haul Truck Drivers
|
N/A |